# Depuy Intl., Ltd. (manufacturer, Leeds, GB): 4 new FDA device listings, incl. bone cement

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Depuy Intl., Ltd. |
| Owner / operator | DePuy Synthes, Inc. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Leeds, GB |
| New listings | 4 |
| Devices | Bone Cement; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented; Bone Cement, Antibiotic; Prosthesis, Hip, Hemi-, Femoral, Metal |
| Product codes | LOD, KWY, MBB, KWL |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| First new listing | 2026-06-15 |
| Latest new listing | 2026-06-15 |
| FDA registration number | 8010379 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.